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Presumed appendiceal abscess discovered to be ruptured Meckel diverticulum following percutaneous drainage

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Abstract

A Meckel diverticulum is an embryonic remnant of the omphalomesenteric duct that occurs in approximately 2% of the population. Most are asymptomatic; however, they are vulnerable to inflammation with subsequent consequences including diverticulitis and perforation. We report an 11-year-old boy who underwent laparoscopic appendectomy for perforated appendicitis at an outside institution. During his convalescence he underwent percutaneous drainage of a presumed postoperative abscess. A follow-up drain study demonstrated an enteric fistula. The drain was slowly removed from the abdomen over a period of 1 week. Three weeks following drain removal the patient reported recurrent nausea and abdominal pain. A CT scan demonstrated a 3.7-cm rim-enhancing air-fluid level with dependent contrast consistent with persistent enteric fistula and abscess. Exploratory laparoscopy was performed, at which time a Meckel diverticulum was identified and resected. This case highlights the diagnostic challenge and limitations of conventional radiology in complicated Meckel diverticulum.

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Correspondence to Daniel J. Ostlie.

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Yang, J.C., Rivard, D.C., Morello, F.P. et al. Presumed appendiceal abscess discovered to be ruptured Meckel diverticulum following percutaneous drainage. Pediatr Radiol 38, 909–911 (2008). https://doi.org/10.1007/s00247-008-0874-1

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  • DOI: https://doi.org/10.1007/s00247-008-0874-1

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